Comparative Effectiveness and Cost-Effectiveness of Colorectal Cancer Screening With Blood-Based Biomarkers (Liquid Biopsy) vs Fecal Tests or Colonoscopy

被引:34
作者
Ladabaum, Uri [1 ,2 ]
Mannalithara, Ajitha [1 ,2 ]
Weng, Yingjie [2 ,3 ]
Schoen, Robert E. [4 ]
Dominitz, Jason A. [5 ,6 ]
Desai, Manisha [2 ,3 ]
Lieberman, David [7 ]
机构
[1] Stanford Univ, Sch Med, Div Gastroenterol & Hepatol, Stanford, CA USA
[2] Stanford Univ, Sch Med, Dept Med, Stanford, CA USA
[3] Stanford Univ, Sch Med, Quantitat Sci Unit, Stanford, CA USA
[4] Univ Pittsburgh, Dept Epidemiol, Div Gastroenterol Hepatol & Nutr, Pittsburgh, PA USA
[5] Vet Adm Puget Sound Hlth Care Syst, Seattle, WA USA
[6] Univ Washington, Sch Med, Dept Med, Div Gastroenterol, Seattle, WA USA
[7] Oregon Hlth & Sci Univ, Div Gastroenterol & Hepatol, Portland, OR USA
关键词
Colorectal Cancer; Screening; Blood-Based Biomarker; Blood-Based Testing; Liquid Biopsy; Comparative Effectiveness; Cost-Effectiveness; Health Economics; Decision Analysis; RISK-STRATIFICATION; FOLLOW-UP; SURVEILLANCE; HEALTH; NEOPLASIA; US; RECOMMENDATIONS; SIGMOIDOSCOPY; MORTALITY; CARE;
D O I
10.1053/j.gastro.2024.03.011
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Colorectal cancer (CRC) screening is highly effective but underused. Blood-based biomarkers (liquid biopsy) could improve screening participation. Methods: Using our established Markov model, screening every 3 years with a blood-based test that meets minimum Centers for Medicare & Medicaid Services' thresholds (CMSmin) (CRC sensitivity 74%, specificity 90%) was compared with established alternatives. Test attributes were varied in sensitivity analyses. Results: CMSmin reduced CRC incidence by 40% and CRC mortality by 52% vs no screening. These reductions were less profound than the 68%-79% and 73%-81%, respectively, achieved with multi-target stool DNA (Cologuard; Exact Sciences) every 3 years, annual fecal immunochemical testing (FIT), or colonoscopy every 10 years. Assuming the same cost as multi-target stool DNA, CMSmin cost $28,500/quality-adjusted life-year gained vs no screening, but FIT, colonoscopy, and multi-target stool DNA were less costly and more effective. CMSmin would match FIT's clinical outcomes if it achieved 1.4- to 1.8-fold FIT's participation rate. Advanced precancerous lesion (APL) sensitivity was a key determinant of a test's effectiveness. A paradigm-changing blood-based test (sensitivity >90% for CRC and 80% for APL; 90% specificity; cost <=$120-$140) would be cost-effective vs FIT at comparable participation. Conclusions: CMSmin could contribute to CRC control by achieving screening in those who will not use established methods. Substituting blood-based testing for established effective CRC screening methods will require higher CRC and APL sensitivities that deliver programmatic benefits matching those of FIT. High APL sensitivity, which can result in CRC prevention, should be a top priority for screening test developers. APL detection should not be penalized by a definition of test specificity that focuses on CRC only.
引用
收藏
页码:378 / 391
页数:14
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